Molecular Cloning of a Novel Member of the GLUT Family of Transporters, SLC2A10 (GLUT10), Localized on Chromosome 20q13.1: A Candidate Gene for NIDDM Susceptibility

By McVie-Wylie A.J.   Lamson D.R.   Chen Y.T.  

Genomics, Vol. 72, Iss. 1, 2001-02 ,pp. : 113-117

Elsevier

Access to resources Recommend Favorite

Molecular Characterization of X-Linked Adrenoleukodystrophy in a Tunisian Family: Identification of a Novel Missense Mutation in the ABCD1 Gene

By  

Neurodegenerative Diseases, Vol. 12, Iss. 4, 2013-05 ,pp. : 207-211

Karger

Access to resources Recommend Favorite

A novel mutation in the MITF gene causes Waardenburg Syndrome Type 2

By Lautenschlager N.T.   Milunsky A.   DeStefano A.   Farrer L.   Baldwin C.T.  

Genetic Analysis: Biomolecular Engineering, Vol. 13, Iss. 2, 1996-07 ,pp. : 43-44

Elsevier

Access to resources Recommend Favorite

Three novel mutations causing a truncated protein within the RP2 gene in Italian families with X-linked retinitis pigmentosa

By De Luca A.   Torrente I.   Mangino M.   Danesi R.   Dallapiccola B.   Novelli G.  

Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Vol. 432, Iss. 3, 2001-01 ,pp. : 79-82

Elsevier

Access to resources Recommend Favorite

Characterization of Novel Promoter and Enhancer Elements of the Mouse Homologue of the Dent Disease Gene, CLCN5, Implicated in X-Linked Hereditary Nephrolithiasis

By Tanaka K.   Fisher S.E.   Craig I.W.  

Genomics, Vol. 58, Iss. 3, 1999-06 ,pp. : 281-292

Elsevier

Access to resources Recommend Favorite